Variant (rsID / SNP)

rs507360

rs507360 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to OR8B3, OR8B2. Location: chromosome 11, position 124,267,177. The table records no clinical significance for this variant.

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Reference-table entries

OR8B3Not classified

Variant type: missense_variant
Chromosome / position: 11:124267177
HGVS: NM_001005467.2,c.71A>G,p.Gln24Arg
Allele change: Missense_Q24R

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.